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  4. NDC Product Code: 63083-2087 Fever Flu Symptom Drops 2087

NDC 63083-2087 Fever Flu Symptom Drops 2087

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63083-2087?
  4. Fever Flu Symptom Drops 2087 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63083-2087
Proprietary Name:
Fever Flu Symptom Drops 2087
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Professional Complementary Health Formulas
Labeler Code:
63083
Product Label ID:
13cfd1c2-95fe-451c-b07e-7d27ad3dfe81
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63083-2087-2

Package Description: 59 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 63083-2087?

The NDC code 63083-2087 is assigned by the FDA to the product Fever Flu Symptom Drops 2087 which is product labeled by Professional Complementary Health Formulas. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63083-2087-2 59 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Fever Flu Symptom Drops 2087?

For the temporary relief of flu-like symptoms such as low-grade fever, chills, nasal or chest congestion, occasional headache, or fatigue.*

Which are Fever Flu Symptom Drops 2087 UNII Codes?

The UNII codes for the active ingredients in this product are:

  • EUPHRASIA STRICTA (UNII: C9642I91WL)
  • EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
  • ULMUS RUBRA BARK (UNII: 91QY4PXU8Q)
  • ULMUS RUBRA BARK (UNII: 91QY4PXU8Q) (Active Moiety)
  • SOLANUM DULCAMARA WHOLE (UNII: G72JA9DHK5)
  • SOLANUM DULCAMARA WHOLE (UNII: G72JA9DHK5) (Active Moiety)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
  • PULSATILLA MONTANA WHOLE (UNII: 24K790T39B)
  • PULSATILLA MONTANA WHOLE (UNII: 24K790T39B) (Active Moiety)
  • EPINEPHRINE (UNII: YKH834O4BH)
  • EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
  • HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE)
  • HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE) (Active Moiety)
  • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
  • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (Active Moiety)
  • AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN)
  • AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN) (Active Moiety)
  • CAMPHOR (NATURAL) (UNII: N20HL7Q941)
  • CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
  • HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I)
  • HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)

Which are Fever Flu Symptom Drops 2087 Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".